Product image of Glyclada (Gliclazide) supplied by GNH India

Glyclada

Active Ingredient:
Gliclazide
Origin:
EU

Glyclada (Gliclazide)

Glyclada is a prescription medication that contains the sulfonylurea agent gliclazide as its active ingredient. It is formulated for oral administration and is marketed in the European Union. As a member of the antidiabetic therapeutic class, Glyclada works by stimulating insulin release from pancreatic beta cells. The product is intended for use under medical supervision in patients with type 2 diabetes mellitus and ongoing management.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Glyclada is indicated for the management of type 2 diabetes mellitus when diet, exercise, and other non‑pharmacologic measures are insufficient to achieve glycemic control.

  • As monotherapy in patients newly diagnosed with type 2 diabetes.
  • In combination with metformin when additional glucose lowering is required.
  • As part of a fixed‑dose combination regimen with other oral antidiabetics.
  • For patients who retain some endogenous insulin secretion.
  • To help achieve target HbA1c levels as determined by a healthcare professional.

Side Effects

The safety profile of Glyclada reflects the typical effects observed with sulfonylurea agents; side effects can range from mild and transient to rare but serious.

Common

  • Mild to moderate hypoglycemia, presenting as shakiness, sweating, or hunger, particularly when meals are delayed.
  • Gastrointestinal discomfort such as nausea, abdominal pain, or dyspepsia.
  • Intermittent headache.
  • Dizziness or a sensation of light‑headedness, often related to low blood glucose.

Serious

  • Severe hypoglycemia with confusion, seizures, or loss of consciousness requiring medical attention.
  • Allergic reactions including rash, itching, urticaria, or facial swelling.
  • Hematologic effects such as reduced white blood cells (leukopenia) or platelets (thrombocytopenia).
  • Hepatic abnormalities reflected by elevated liver enzymes or jaundice.

Precautions & Warnings

Before starting Glyclada, healthcare providers should evaluate several clinical factors to minimize risks and ensure appropriate use.

  • Assess renal and hepatic function, as impairment may affect drug clearance.
  • Review history of cardiovascular disease, since sulfonylureas can influence cardiac outcomes.
  • Confirm that the patient has sufficient endogenous insulin production.
  • Caution in elderly patients due to increased susceptibility to hypoglycemia.
  • Advise patients to avoid alcohol excess, which can potentiate hypoglycemic episodes.
  • Discuss pregnancy and lactation status; safety data are limited.

Avoid Interactions

Glyclada may interact with other medicines, altering blood glucose levels or increasing the risk of adverse effects.

Avoid

  • Concomitant use with other sulfonylureas or insulin that can cause severe hypoglycemia.
  • Strong CYP2C9 inhibitors (e.g., fluconazole, amiodarone) that may raise gliclazide concentrations.

Use with caution

  • Beta‑blockers, which can mask hypoglycemia symptoms.
  • Thiazide diuretics, which may affect glucose tolerance.
  • Anticoagulants, as glycemic fluctuations can influence INR stability.
  • Oral contraceptives, which might modify gliclazide metabolism.

Frequently Asked Questions

Glyclada contains gliclazide, a sulfonylurea that binds to the sulfonylurea receptor on pancreatic beta cells, closes ATP‑sensitive potassium channels, and promotes glucose‑dependent insulin release.

Glyclada is primarily prescribed for the treatment of type 2 diabetes mellitus when lifestyle measures alone do not achieve adequate blood glucose control.

Yes, Glyclada may be combined with metformin to provide additional glucose‑lowering effect when monotherapy is insufficient, under the guidance of a healthcare professional.

Common side effects include mild hypoglycemia, gastrointestinal discomfort such as nausea or abdominal pain, headache, and occasional dizziness.

Serious reactions include severe hypoglycemia with confusion or loss of consciousness, allergic skin reactions, blood cell count abnormalities, and signs of liver dysfunction.

Renal function should be evaluated before initiating Glyclada; dose adjustment or alternative therapy may be needed in patients with significant renal impairment.

The safety of Glyclada in pregnancy has not been established; it should only be used if the potential benefit justifies the potential risk to the fetus.

Excessive alcohol can increase the risk of hypoglycemia when taking Glyclada, so patients are advised to limit alcohol intake.

Concurrent use of other sulfonylureas, insulin, or strong CYP2C9 inhibitors should be avoided because they can markedly increase the risk of hypoglycemia.

Beta‑blockers can be used with Glyclada, but they may mask the typical symptoms of hypoglycemia, so patients should monitor blood glucose closely.

Elderly patients are more prone to hypoglycemia; careful dose titration and regular glucose monitoring are recommended.

Baseline assessments typically include fasting plasma glucose, HbA1c, renal and hepatic function tests, and a review of cardiovascular status.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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